Canonical Allele Identifier: CA2320559237
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6697820A= , CM000681.2:g.6697820A= GRCh38
NC_000019.9:g.6697831A= , CM000681.1:g.6697831A= GRCh37
NC_000019.8:g.6648831A= NCBI36
NG_009557.1:g.27832T= , LRG_27:g.27832T=

Transcript Alleles

HGVS Amino-acid change
ENST00000695651.1:n.789-26T=
ENST00000695652.1:c.2318-26T= ENSP00000512083.1:n.2318-26T=
ENST00000695653.1:c.350-26T= ENSP00000512084.1:n.350-26T=
ENST00000695654.1:c.1565-26T= ENSP00000512085.1:n.1565-26T=
ENST00000695655.1:c.1382-26T= ENSP00000512086.1:n.1382-26T=
ENST00000695692.1:n.1805-26T=
ENST00000245907.11:c.2441-26T= MANE Select ENSP00000245907.4:n.2441-26T=
ENST00000245907.10:c.2441-26T= ENSP00000245907.4:n.2441-26T=
ENST00000602053.1:n.489-26T=
NM_000064.3:c.2441-26T= NP_000055.2:n.2441-26T=
NM_000064.4:c.2441-26T= MANE Select NP_000055.2:n.2441-26T=